| | | Single nucleotide variant (nonsense) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Insertion (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Deletion (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (nonsense) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Deletion (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Deletion (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Duplication (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Deletion (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Deletion (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (nonsense) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Deletion (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (splice donor variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Indel (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Neonatal severe primary hyperparathyroidism | |
| | | Single nucleotide variant (splice donor variant) | Familial hypocalciuric hypercalcemia +3 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (splice donor variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Insertion (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Deletion (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (nonsense) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (nonsense) | Familial hypocalciuric hypercalcemia +2 more | |
| | | Deletion (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +2 more | |
| | | Deletion (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Deletion (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Deletion (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Deletion (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Duplication (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (nonsense) | CASR-related condition +3 more | |
| | | Deletion | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Familial hypocalciuric hypercalcemia +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant hypocalcemia 1 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant hypocalcemia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (nonsense) | Neonatal severe primary hyperparathyroidism +5 more | |
| | | Microsatellite (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Autosomal dominant hypocalcemia 1 +2 more | |
| | | Indel (frameshift variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (nonsense) | Familial hypocalciuric hypercalcemia +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +2 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, idiopathic generalized, susceptibility to, 8 +5 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant hypocalcemia 1 +2 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +2 more | GPathogenic/Likely pathogenic |
| | | Indel (missense variant) | Familial hypocalciuric hypercalcemia +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +2 more | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant hypocalcemia 1 +5 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Familial hypocalciuric hypercalcemia +2 more | |
| | | Single nucleotide variant (nonsense) | Nephrolithiasis/nephrocalcinosis +4 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +4 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +10 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant hypocalcemia 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Nephrolithiasis/nephrocalcinosis +8 more | |
| | | Deletion (frameshift variant) | Autosomal dominant hypocalcemia 1 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +3 more | |
| | | Deletion (frameshift variant) | Autosomal dominant hypocalcemia 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal dominant hypocalcemia +5 more | |
| | | Single nucleotide variant (nonsense) | Familial hypocalciuric hypercalcemia +2 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal dominant hypocalcemia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant hypocalcemia 1 +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | CASR-related condition +6 more | |
| | | Single nucleotide variant (missense variant) | Familial hypocalciuric hypercalcemia +2 more | |
| | | Single nucleotide variant (missense variant) | CASR-related condition +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |